Variant #0001002366 (NC_000016.9:g.4405148G>A, NM_024535.4:c.*11C>T (CORO7))

Chromosome 16
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.4405148G>A
DNA change (hg38) -
Published as CORO7(NM_024535.4):c.*11C>T (p.?)
ISCN -
DB-ID CORO7_000034
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CORO7-PAM16 NM_001201479.1 ?/. - c.2772+139C>T r.(=) p.(=)
PAM16 NM_016069.9 ?/. - c.-3913C>T r.(?) p.(=)
CORO7 NM_024535.4 ?/. - c.*11C>T r.(=) p.(=)
VASN NM_138440.2 ?/. - c.-16856G>A r.(?) p.(=)


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